DNA polymerases δ and E (Polδ and PolE) are widely thought to be the major DNA polymerases that function in elongation during DNA replication in eukaryotic cells. However, the precise roles of these polymerases are still unclear. Here we comparatively analysed DNA replication in Xenopus egg extracts in which Polδ or PolE was immunodepleted. Depletion of either polymerase resulted in a significant decrease in DNA synthesis and accumulation of short nascent DNA products, indicating an elongation defect. Moreover, Polδ depletion caused a more severe defect in elongation, as shown by sustained accumulation of both short nascent DNA products and single-stranded DNA gaps, and also by elevated chromatin binding of replication proteins that function more frequently during lagging strand synthesis. Therefore, our data strongly suggest the possibilities that Polδ is essential for lagging strand synthesis and that this function of Polδ cannot be substituted for by PolE. © Blackwell Publishing Limited.
CITATION STYLE
Fukui, T., Yamauchi, K., Muroya, T., Akiyama, M., Maki, H., Sugino, A., & Waga, S. (2004). Distinct roles of DNA polymerases delta and epsilon at the replication fork in Xenopus egg extracts. Genes to Cells, 9(3), 179–191. https://doi.org/10.1111/j.1356-9597.2004.00716.x
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